Publications by authors named "Donald R Blake"

Article Synopsis
  • Initial efforts in Hong Kong have effectively controlled primary air pollutants; however, ozone levels have risen over the past 30 years, indicating a need to address volatile organic compounds (VOCs), which are key precursors to ozone.
  • A study conducted from May 2015 to June 2019 assessed VOC concentrations at roadside, suburban, and rural sites, revealing that roadside areas had the highest TVOC levels (23.05 ppbv), followed by suburban (12.68 ppbv) and rural (5.16 ppbv) locations.
  • The research identified various sources of VOCs at these sites using the Positive Matrix Factorization model, with LPG and gasoline evaporation being significant contributors in urban areas, while aged air mass and
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  • Wildfires are a growing contributor to air pollution, particularly due to reactive organic compounds (ROC), which have varying health impacts based on their toxicity and abundance.
  • A study combining field campaign data and air quality modeling found that current emissions estimates capture only 40-45% of the total ROC released from wildfires.
  • The research indicates that particulate ROC could significantly affect health risks from smoke exposure, highlighting the need for more accurate toxicity data on these compounds.
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Climate impacts of landfill gas emissions were investigated for 20- and 100-year time horizons to identify the effects of atmospheric lifetimes of short- and long-lived drivers. Direct and indirect climate impacts were determined for methane and 79 trace species. The impacts were quantified using global warming potential, GWP (direct and indirect); atmospheric degradation (direct); tropospheric ozone forming potential (indirect); secondary aerosol forming potential (indirect) and stratospheric ozone depleting potential (indirect).

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Electronic cigarette smoking (or vaping) is on the rise, presenting questions about the effects of secondhand exposure. The chemical composition of vape emissions was examined in the exhaled breath of eight human volunteers with the high chemical specificity of complementary online and offline techniques. Our study is the first to take multiple exhaled puff measurements from human participants and compare volatile organic compound (VOC) concentrations between two commonly used methods, proton-transfer-reaction time-of-flight mass spectrometry (PTR-ToF-MS) and gas chromatography (GC).

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We use global airborne observations of propane (CH) and ethane (CH) from the Atmospheric Tomography (ATom) and HIAPER Pole-to-Pole Observations (HIPPO), as well as U.S.-based aircraft and tower observations by NOAA and from the NCAR FRAPPE campaign as tracers for emissions from oil and gas operations.

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The role of anthropogenic NO emissions in secondary organic aerosol (SOA) production is not fully understood but is important for understanding the contribution of emissions to air quality. Here, we examine the role of organic nitrates (RONO) in SOA formation over the Korean Peninsula during the Korea-United States Air Quality field study in Spring 2016 as a model for RONO aerosol in cities worldwide. We use aircraft-based measurements of the particle phase and total (gas + particle) RONO to explore RONO phase partitioning.

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Oceans emit large quantities of dimethyl sulfide (DMS) to the marine atmosphere. The oxidation of DMS leads to the formation and growth of cloud condensation nuclei (CCN) with consequent effects on Earth's radiation balance and climate. The quantitative assessment of the impact of DMS emissions on CCN concentrations necessitates a detailed description of the oxidation of DMS in the presence of existing aerosol particles and clouds.

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Formic acid (HCOOH) is an important component of atmospheric acidity but its budget is poorly understood, with prior observations implying substantial missing sources. Here we combine pole-to-pole airborne observations from the Atmospheric Tomography Mission (ATom) with chemical transport model (GEOS-Chem CTM) and back trajectory analyses to provide the first global in-situ characterization of HCOOH in the remote atmosphere. ATom reveals sub-100 ppt HCOOH concentrations over most of the remote oceans, punctuated by large enhancements associated with continental outflow.

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Since 2012, studies in mice, rats, and humans have suggested that abnormalities in purinergic signaling may be a final common pathway for many genetic and environmental causes of autism spectrum disorder (ASD). The current study in mice was conducted to characterize the bioenergetic, metabolomic, breathomic, and behavioral features of acute hyperpurinergia triggered by systemic injection of the purinergic agonist and danger signal, extracellular ATP (eATP). Responses were studied in C57BL/6J mice in the maternal immune activation (MIA) model and controls.

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  • The global oxidation capacity, measured by hydroxyl radicals (OH), affects the lifespan of gases like methane and carbon monoxide, with models generally underestimating their lifetimes due to excessive OH levels.
  • Observations from NASA's ATom campaign provide insights into remote ocean oxidation capacity, showing that the GEOS-Chem model accurately reflects remote OH profiles but struggles with seasonal NO estimates.
  • The study reveals an unexplained enhancement of OH reactivity below 3 km during ATom-1, indicating potential missing reactive VOCs that existing models fail to account for.
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  • Global coupled chemistry-climate models tend to underestimate carbon monoxide (CO) levels in the Northern Hemisphere, especially peaking in late winter and early spring, which is linked to factors beyond just emissions from human activity and biomass burning.
  • A study using data from the KORUS-AQ experiment revealed that CO was underestimated by 42% in a control scenario, while using satellite data assimilation reduced this bias significantly.
  • Adjusting CO emissions in models not only improved CO accuracy but also positively impacted related compounds such as ozone and hydroxyl (OH), indicating that better accounting for anthropogenic sources enhances overall air quality modeling.
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Investigating the long-term trends of alkyl nitrates (RONO) is of great importance for evaluating the variations of photochemical pollution. Mixing ratios of C-C RONO were measured in autumn Hong Kong from 2002 to 2016, and the average level of 2-butyl nitrate (2-BuONO) always ranked first. The C-C RONO all showed increasing trends (p < 0.

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In order to improve local air quality of Hong Kong, more than 99% taxies and public light buses were changed from diesel to liquefied petroleum gas (LPG) fuel type in the early 2000s. In addition to the catalytic converters wear and tear, it is necessary to control air pollutants emitted from LPG vehicles. Therefore, an LPG catalytic converter replacement programme (CCRP) was fulfilled from October 2013 to April 2014 by the Hong Kong government.

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Dimethyl sulfide (DMS), emitted from the oceans, is the most abundant biological source of sulfur to the marine atmosphere. Atmospheric DMS is oxidized to condensable products that form secondary aerosols that affect Earth's radiative balance by scattering solar radiation and serving as cloud condensation nuclei. We report the atmospheric discovery of a previously unquantified DMS oxidation product, hydroperoxymethyl thioformate (HPMTF, HOOCHSCHO), identified through global-scale airborne observations that demonstrate it to be a major reservoir of marine sulfur.

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We apply a high-resolution chemical transport model (GEOS-Chem CTM) with updated treatment of volatile organic compounds (VOCs) and a comprehensive suite of airborne datasets over North America to (i) characterize the VOC budget and (ii) test the ability of current models to capture the distribution and reactivity of atmospheric VOCs over this region. Biogenic emissions dominate the North American VOC budget in the model, accounting for 70 % and 95 % of annually emitted VOC carbon and reactivity, respectively. Based on current inventories anthropogenic emissions have declined to the point where biogenic emissions are the dominant summertime source of VOC reactivity even in most major North American cities.

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We report airborne measurements of acetaldehyde (CHCHO) during the first and second deployments of the National Aeronautics and Space Administration (NASA) Atmospheric Tomography Mission (ATom). The budget of CHCHO is examined using the Community Atmospheric Model with chemistry (CAM-chem), with a newly-developed online air-sea exchange module. The upper limit of the global ocean net emission of CHCHO is estimated to be 34 Tg a (42 Tg a if considering bubble-mediated transfer), and the ocean impacts on tropospheric CHCHO are mostly confined to the marine boundary layer.

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Rapid increase in atmospheric methane (CH) mixing ratios over the past century is attributable to the intensification of human activities. Information on spatially explicit source contributions is needed to develop efficient and cost-effective CH emission reduction and mitigation strategies to addresses near-term climate change. This study collected long-term ambient CH measurements at Mount Wilson Observatory (MWO) in Los Angeles, California, to estimate the annual CH emissions from the portion of Los Angeles County that is within the South Coast Air Basin (SCLA).

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Alkyl nitrates (RONO) are important reservoirs of nitrogen oxides and play key roles in the tropospheric chemistry. Two phases of intensive campaigns were conducted during February-April and June-July of 2017 at a rural coastal site and in open oil fields of the Yellow River Delta region, northern China. C-C alkyl nitrates showed higher concentration levels in summer than in winter-spring (p < 0.

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Article Synopsis
  • The concentration of nitrogen oxides (NO) is crucial for monitoring air quality, primarily being transformed into HNO through oxidation.
  • Recent studies suggest that particle-phase HNO may photolyze much faster than gas-phase HNO, potentially affecting our understanding of NO and HNO dynamics.
  • Observations from the KORUS-AQ study indicate that the rate of photolysis for particle-phase HNO is likely only moderately faster than gas-phase, which aligns with existing data and may help interpret the behavior of HONO and NO in aged air.
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Emissions of twelve (hydro)chlorofluorocarbons (F-gases) and methane were quantified using large-scale static chambers as a function of cover type (daily, intermediate, final) and seasonal variation (wet, dry) at a California landfill. The majority of the F-gas fluxes was positive and varied over 7 orders of magnitude across the cover types in a given season (wet: 10 to 10 g/m-day; dry: 10 to 10 g/m-day). The highest fluxes were from active filling areas with thin, coarse-grained daily covers, whereas the lowest fluxes were from the thick, fine-grained final cover.

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Oil and gas (O&G) facilities emit air pollutants that are potentially a major health risk for nearby populations. We characterized prenatal through adult health risks for acute (1 h) and chronic (30 year) residential inhalation exposure scenarios to nonmethane hydrocarbons (NMHCs) for these populations. We used ambient air sample results to estimate and compare risks for four residential scenarios.

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This work reports the first ground-based atmospheric measurements of 26 halocarbons in Singapore, an urban-industrial city-state in Southeast (SE) Asia. A total of 166 whole air canister samples collected during two intensive 7 Southeast Asian Studies (7SEAS) campaigns (August-October 2011 and 2012) were analyzed for C-C halocarbons using gas chromatography-electron capture/mass spectrometric detection. The halocarbon dataset was supplemented with measurements of selected non-methane hydrocarbons (NMHCs), C-C alkyl nitrates, sulfur gases and carbon monoxide to better understand sources and atmospheric processes.

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In the efforts at controlling automobile emissions, it is important to know in what extent air pollutants from on-road vehicles could be truly reduced. In 2014 we conducted tests in a heavily trafficked tunnel in south China to characterize emissions of volatile organic compounds (VOC) from on-road vehicle fleet and compared our results with those obtained in the same tunnel in 2004. Alkanes, aromatics, and alkenes had average emission factors (EFs) of 338, 63, and 42 mg km in 2014 against that of 194, 129, and 160 mg km in 2004, respectively.

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Volatile organic compounds (VOCs) measured from exhaled breath have great promise for the diagnosis of bacterial infections. However, determining human or microbial origin of VOCs detected in breath remains a great challenge. For example, the microbial fermentation product 2,3-butanedione was recently found in the breath of Cystic Fibrosis (CF) patients; parallel culture-independent metagenomic sequencing of the same samples revealed that Streptococcus and Rothia spp.

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